Abstract

BackgroundALS patients have changed peripheral immunity. It is unknown whether peripheral immunity is related to cognitive dysfunction in ALS patients.ObjectiveTo explore the relationship between the peripheral blood lymphocyte subsets and the cognitive status in ALS patients.MethodsAmong 81 ALS patients, we compared the demographic, clinical, and peripheral levels of total T lymphocyte, CD4+ T lymphocyte, CD8+ T lymphocyte, B lymphocyte, and NK cell between those with cognitive impairment (ALS-ci) and those without (ALS-nci). The cognitive status was evaluated via the Chinese version of the Edinburgh cognitive and behavioral screen (ECAS). Significant predictors of cognitive impairment in univariate logistic regression analysis were further examined using multivariate logistic regression analysis.Results39.5% of all ALS patients had cognitive impairment. The ALS-ci group had shorter education time, older age at both symptom onset and testing, longer disease duration, and lower levels of peripheral total, CD4+, and CD8+ T lymphocyte and B lymphocyte than the ALS-nci group. Frequency of behavioral impairment did not differ between the two groups. While parameters with significant differences identified by group comparison were also significant predictors of cognitive impairment in univariate logistic regression analysis except the level of B lymphocyte, only older age at testing, education time less than 9 years, and lower level of CD4+ T lymphocyte remained significant in multivariate logistic regression analysis. The predictive model combining these three parameters had an area under the receiver operating characteristic curve value of 0.842 with a sensitivity of 90.6% and a specificity of 67.3%.ConclusionIn Chinese ALS patients, blood CD4+ T lymphocyte might help evaluate cognitive impairment along with age and education level.

Highlights

  • Amyotrophic lateral sclerosis (ALS) is a fatal and progressive neurodegenerative disease characterized by loss of upper and lower motor neurons [1]

  • Two patients in the ALS-ci group and three patients in the ALS patients had no cognitive impairment (ALS-nci) group did not have the behavioral part of Edinburgh cognitive and behavioral screen (ECAS) since they were neither accompanied by caregivers during hospitalization nor had they close contacts during post-hospitalization call. 3 (10%) patients had disinhibition, 6 (20.0%) patients had apathy, 5 (16.7%) patients had loss of sympathy, 1 (3.3%) patient had perseveration, and 2 (6.7%) patients had changes in eating behaviour in the ALS-ci group, while 1 (2.2%) patient had disinhibition, 4 (8.7%) patients had apathy, 4 (8.7%) patients had loss of sympathy, 2 (4.3%) patients had perseveration, and 2 (4.3%) patients had changes in eating behaviour in the ALS-nci group

  • Our study showed that ALS patients with cognitive impairment (ALS-ci group) displayed a different peripheral immune profile compared to those without (ALS-nci group)

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Summary

Introduction

Amyotrophic lateral sclerosis (ALS) is a fatal and progressive neurodegenerative disease characterized by loss of upper and lower motor neurons [1]. It is of great importance to accurately identify the cognitive status of ALS patients. At present, this process largely relies on comprehensive neuropsychological assessment [11]. In ALS patients, studies have detected deficits in various cognitive domains including executive function, social cognition, language, and working memory [11]. The Edinburgh cognitive and behavioral screen (ECAS), a rapid neuropsychological screening tool, was developed to identify cognitive and behavioral changes of ALS patients [13]. ECAS has been widely implemented in both clinical and research settings with different language versions and has proven to be an efficient and reliable screening tool for ALS patients [12, 14,15,16,17,18]. It is unknown whether peripheral immunity is related to cognitive dysfunction in ALS patients

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